Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1644008

FEI Number

1000117494

Entity Name

Newview Oklahoma, Inc

City/State/Country

Oklahoma City, OK, US

Establishment Address

501 N Douglas Avenue, Oklahoma City, OK 73106, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

NewView Oklahoma (Owner Number: 10035470)

Owner / Operator Contact Address

501 N. Douglas Avenue, Oklahoma City, OK 73106, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dukal Goodsense Curaplex Medline Coflex Med Aplicare Honeywell Genuine First Aid Flexpak Kerlix Medi-First Curity Berrcom First Care Best Health, Burnfree Cambridge Sensors IvyX Medica McKesson Medical Industries Grafco AMBU Dynarex

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRR	First Aid Kit With Drug	Unknown	Class N	N/A	2011-03-14

Official Correspondent

Linda Gigger

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NewView Oklahoma

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1644008. Last updated year: 2026. Please use registration number 1644008 when referencing this establishment in official correspondence.